HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenacyl bromide → 2-(3,5-Dichlorophenyl)oxirane
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenacyl bromide | HCID 6259 | — |
| Edukt | Styrene Oxide | HCID 7276 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 3',5'-Dichloroacetophenone | HCID 2758058 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 2-(3,5-Dichlorophenyl)oxirane | HCID 13488795 | — |
Reaktionsschritte
The phenacyl bromide intermediate for the above-mentioned styrene oxide is prepared by brominating 10 g of 3,5-dichloroacetophenone in 50 ml of CHCl3 /50 ml of EtOAc with 23.6 g of CuBr2. The mixture is heated at reflux for 2.5 hours and cooled to room temperature. After stirring for 16 hours at room temperature, the mixture is cooled in ice for 2 hours and filtered. The filter cake is washed with 50 ml of CHCl3 and the combined filtrates are twice decolorized with activated carbon, filtered, and evaporated to dryness in vacuo to afford the orange oil of the 3,5-dichlorostyrene oxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04407819 |
| Quelldatensatz | uspto-grants-1983_10 |
| ORD ID | ord-acc0afc7627a4a26ab50c75c81da3f4d |
| Quellennotiz | uspto-grants-1983_10 |